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IRB Home > Forms & Consent Templates > NonMedical

  Social & Behavioral Research: Forms & Consent Templates

This section contains all of the forms and consent templates that apply to investigators from:

  • Business
  • Education
  • Engineering
  • Humanities & Sciences
  • Law
  • Psychology (except MRI studies)

*Please note that when creating a protocol for IRB submission, these investigators need to select the Non-Medical eProtocol Application category.

* Any study that involves the collection and analyses of human biological specimens and/or Protected Health Information (PHI) will need to be submitted on the Medical eProtocol application.

For questions, please contact the Non-Medical IRB Panel Staff

Templates:

   Consents
        See consent template updates for recent changes
Consent
doc
02/23/16
Research Information Sheet - Use for Waiver of Documentation
doc
1/7/15
Parent or Legally Authorized Representative Permission
doc
02/23/16
Video Use Consent
doc
02/23/16
   Assents, phone screens, scripts
        See consent template updates for recent changes
Assent – under 18
doc
1/7/15
Assent – adults (18+) unable to provide consent i.e., LAR provides consent
doc
1/7/15
Telephone Screening of Potential Subjects
  • Sample Phone Screen Level 1a
  • Sample Phone Screen Level 1b
Oral Consent Script
doc
12/16/13


Other Forms:

    HS Research Determination; Other
Human Subject Research (HSR) Determination Form
Letter of Agreement - for research in cooperation with other organizations

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    Scientific Review
Review of Scientific and Scholarly Validity, and Oversight (by Academic Sponsor)
Review of Scientific and Scholarly Validity (by Dept Chair or School Dean)

 

eProtocol Forms:

   Required Attachments
International Research Supplemental Questions – research outside the US
DOE-supported research: Protection of Personally Identifiable Information (PII)    [Form APP-14]
  Sample eProtocol Application Forms

      New, Modification, Continuing Review

  (These are for informational purposes only)
New:
    -Regular
    -Expedited
    -Exempt
Mod
ContRev
eProtocol is used to submit:
  • New Protocol applications - see examples above.
      - Complete and attach supplemental required attachments as needed (see above)
  • Modifications to approved protocols (need prior IRB approval to implement).
  • Continuing Review applications.
  • Reports unanticipated problems, events/information requiring prompt reporting.
  • Final Reports (not required for Exempt research).

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